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1:
H
ome
(ALT-H)
2:
H
M
A Joint
(ALT-M)
3:
H
u
man Medicines
(ALT-U)
4:
V
eterinary Medicines
(ALT-V)
4.1:
H
e
ads of Agencies
(ALT-E)
4.2:
C
MDv
(ALT-C)
4.3:
VM
R
I Product Index
(ALT-R)
4.4:
D
i
rectory
(ALT-I)
You are here:
Veterinary Medicines
>
CMDv
>
CMDv guidance
> General Info on Licensing System
4.2.1:
Ab
o
ut CMDv, Activities
(ALT-O)
4.2.2:
CMDv
g
uidance
(ALT-G)
4.2.2.1:
Ge
n
eral Info on Licensing System
(ALT-N)
4.2.2.2:
A
p
plications
(ALT-P)
4.2.2.3:
Mar
k
eting Authorisation procedures
(ALT-K)
4.2.2.4:
Varia
t
ions
(ALT-T)
4.2.2.5:
Rene
w
als
(ALT-W)
4.2.2.6:
Referra
l
s
(ALT-L)
4.2.2.7:
S
PC, Labelling and Package leaflet
(ALT-S)
4.2.2.8:
Miscellaneous
4.2.3:
Pharmacovigilance
4.2.4:
Reports for Release
4.2.5:
4.2.6:
Special topics
4.2.7:
Statistics
4.2.8:
Calendar
4.2.9:
Fre
q
uently asked questions
(ALT-Q)
4.2.10:
Contact Form
4.2.11:
submission of translations
4.2.12:
What's new Archive (
6
months)
(ALT-6)
Transfer of information contained in Notice to Applicants, Volume 6A, Chapter 7 (Nov 2012)
CMDv GUI-22 Format and no. of copies for new MAAs
CMDv GUI-23 Format and no. of copies post-authorisation procedures
CMDv GUI-25 Payment terms & addresses for national fees
CMDv GUI-26 Addresses for delivery of dossier
CMDv GUI-27 Packaging ‘blue-box’ requirements in
MRP
/
DCP
CMDv GUI-28 Dossier languages
CMDv GUI-29 List of national official journals
CMDv GUI-30 Product samples for visual/laboratory control by
NCAs
